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Novel approach to classifying patients with pulmonary arterial hypertension using cluster analysis

Pulmonary arterial hypertension (PAH) patients have distinct disease courses and responses to treatment, but current diagnostic and treatment schemes provide limited insight. We aimed to see if cluster analysis could distinguish clinical phenotypes in PAH. An unbiased cluster analysis was performed...

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Autores principales: Parikh, Kishan S., Rao, Youlan, Ahmad, Tariq, Shen, Kai, Felker, G. Michael, Rajagopal, Sudarshan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467940/
https://www.ncbi.nlm.nih.gov/pubmed/28597780
http://dx.doi.org/10.1177/2045893217705891
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author Parikh, Kishan S.
Rao, Youlan
Ahmad, Tariq
Shen, Kai
Felker, G. Michael
Rajagopal, Sudarshan
author_facet Parikh, Kishan S.
Rao, Youlan
Ahmad, Tariq
Shen, Kai
Felker, G. Michael
Rajagopal, Sudarshan
author_sort Parikh, Kishan S.
collection PubMed
description Pulmonary arterial hypertension (PAH) patients have distinct disease courses and responses to treatment, but current diagnostic and treatment schemes provide limited insight. We aimed to see if cluster analysis could distinguish clinical phenotypes in PAH. An unbiased cluster analysis was performed on 17 baseline clinical variables of PAH patients from the FREEDOM-M, FREEDOM-C, and FREEDOM-C2 randomized trials of oral treprostinil versus placebo. Participants were either treatment-naïve (FREEDOM-M) or on background therapy (FREEDOM-C, FREEDOM-C2). We tested for association of clusters with outcomes and interaction with respect to treatment. Primary outcome was 6-minute walking distance (6MWD) change. We included 966 participants with 12-week (FREEDOM-M) or 16-week (FREEDOM-C and FREEDOM-C2) follow-up. Four patient clusters were identified. Compared with Clusters 1 (n = 131) and 2 (n = 496), Clusters 3 (n = 246) and 4 (n = 93) patients were older, heavier, had worse baseline functional class, 6MWD, Borg Dyspnea Index, and fewer years since PAH diagnosis. Clusters also differed by PAH etiology and background therapies, but not gender or race. Mean treatment effect of oral treprostinil differed across Clusters 1–4 increased in a monotonic fashion (Cluster 1: 10.9 m; Cluster 2: 13.0 m; Cluster 3: 25.0 m; Cluster 4: 50.9 m; interaction P value = 0.048). We identified four distinct clusters of PAH patients based on common patient characteristics. Patients who were older, diagnosed with PAH for a shorter period, and had worse baseline symptoms and exercise capacity had the greatest response to oral treprostinil treatment.
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spelling pubmed-54679402017-06-20 Novel approach to classifying patients with pulmonary arterial hypertension using cluster analysis Parikh, Kishan S. Rao, Youlan Ahmad, Tariq Shen, Kai Felker, G. Michael Rajagopal, Sudarshan Pulm Circ Research Articles Pulmonary arterial hypertension (PAH) patients have distinct disease courses and responses to treatment, but current diagnostic and treatment schemes provide limited insight. We aimed to see if cluster analysis could distinguish clinical phenotypes in PAH. An unbiased cluster analysis was performed on 17 baseline clinical variables of PAH patients from the FREEDOM-M, FREEDOM-C, and FREEDOM-C2 randomized trials of oral treprostinil versus placebo. Participants were either treatment-naïve (FREEDOM-M) or on background therapy (FREEDOM-C, FREEDOM-C2). We tested for association of clusters with outcomes and interaction with respect to treatment. Primary outcome was 6-minute walking distance (6MWD) change. We included 966 participants with 12-week (FREEDOM-M) or 16-week (FREEDOM-C and FREEDOM-C2) follow-up. Four patient clusters were identified. Compared with Clusters 1 (n = 131) and 2 (n = 496), Clusters 3 (n = 246) and 4 (n = 93) patients were older, heavier, had worse baseline functional class, 6MWD, Borg Dyspnea Index, and fewer years since PAH diagnosis. Clusters also differed by PAH etiology and background therapies, but not gender or race. Mean treatment effect of oral treprostinil differed across Clusters 1–4 increased in a monotonic fashion (Cluster 1: 10.9 m; Cluster 2: 13.0 m; Cluster 3: 25.0 m; Cluster 4: 50.9 m; interaction P value = 0.048). We identified four distinct clusters of PAH patients based on common patient characteristics. Patients who were older, diagnosed with PAH for a shorter period, and had worse baseline symptoms and exercise capacity had the greatest response to oral treprostinil treatment. SAGE Publications 2017-05-12 /pmc/articles/PMC5467940/ /pubmed/28597780 http://dx.doi.org/10.1177/2045893217705891 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Articles
Parikh, Kishan S.
Rao, Youlan
Ahmad, Tariq
Shen, Kai
Felker, G. Michael
Rajagopal, Sudarshan
Novel approach to classifying patients with pulmonary arterial hypertension using cluster analysis
title Novel approach to classifying patients with pulmonary arterial hypertension using cluster analysis
title_full Novel approach to classifying patients with pulmonary arterial hypertension using cluster analysis
title_fullStr Novel approach to classifying patients with pulmonary arterial hypertension using cluster analysis
title_full_unstemmed Novel approach to classifying patients with pulmonary arterial hypertension using cluster analysis
title_short Novel approach to classifying patients with pulmonary arterial hypertension using cluster analysis
title_sort novel approach to classifying patients with pulmonary arterial hypertension using cluster analysis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467940/
https://www.ncbi.nlm.nih.gov/pubmed/28597780
http://dx.doi.org/10.1177/2045893217705891
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